The order in which job vacancies are displayed is determined by a composite score based on the following factors:
Keyword Relevance: How well your search terms match the vacancy details. We prioritize matches found in the job title, followed by job requirements, location names, and educational levels. Matches within general employer information or the organization's name carry a lower weight.
Commercial Prioritization (Premium Jobs): Vacancies paid for by employers ('Premium' or 'Sponsored') receive a ranking boost and will appear higher in the search results.
Recency (Date Relevance): Newer vacancies are prioritized. The relevance score of a vacancy is reduced by half once the posting is older than 30 days.
Proximity (Distance Relevance): Vacancies located closer to your search location are ranked higher. For vacancies located more than 30 km from the search center, the relevance score is halved.
The final ranking is established by multiplying all these individual factors to calculate the total relevance score.
We are looking for a skilled and driven Formulation Development Scientist to join our UK manufacturing site. This role acts as the critical technical bridge between our India-based R&D centre and the UK Technology Transfer (TT) department, supporting the seamless transition of liquid products from development through to commercial manufacturing.
Key Responsibilities
* Lead and support pilot batch manufacturing, scale-up batches, and troubleshooting of commercial batch failures at the UK site.
* Serve as the primary technical liaison between the India R&D team and the UK TT department, ensuring effective knowledge transfer and alignment on formulation strategies.
* Execute and oversee technology transfer activities for oral liquid and suspension products, ensuring compliance with regulatory requirements and internal quality standards.
* Develop and optimize homogenisation processes for large-volume liquid products, ensuring product uniformity, stability, and consistency at scale.
* Prepare and review technical documents including batch manufacturing records, technology transfer reports, process descriptions, and deviation investigations.
* Identify root causes of manufacturing issues and implement robust corrective and preventive actions (CAPAs).
* Collaborate cross-functionally with QA, QC, Regulatory Affairs, and Manufacturing teams to support product lifecycle activities.
* Contribute to process validation, equipment qualification, and process analytical technology (PAT) initiatives as applicable.
* Stay current with regulatory guidelines (ICH, MHRA, EMA) relevant to liquid dosage form development and manufacturing.
Qualifications & Experience
Education
* M.Pharm / M.Sc. in Pharmaceutics, Pharmaceutical Sciences, or a closely related discipline.
* Ph.D. is an advantage but not mandatory.
Experience
* 6-12 years of hands-on experience in pharmaceutical formulation development, with a focus on oral liquids and suspensions.
* Demonstrated experience in scale-up and technology transfer of liquid dosage forms.
* Practical experience with homogenisation equipment (high-shear mixers, rotor-stator homogenisers) at pilot and commercial scale.
* Prior exposure to a cross-site or cross-functional TT role is highly desirable.
Technical Skills
* Strong understanding of formulation principles for oral liquids and suspensions (rheology, particle size, physicochemical stability).
* Familiarity with ICH Q8/Q9/Q10 guidelines and QbD principles.
* Experience with GMP manufacturing environments and documentation practices.
* Working knowledge of relevant regulatory frameworks (MHRA, EMA, ANDA/CTD as applicable).
Soft Skills
* Strong communication skills — able to operate effectively across geographies and functions.
* Analytical and structured problem-solving mindset.
* Self-driven with the ability to manage multiple priorities independently.
* Collaborative team player with a proactive approach